Header Module
Protocol ID ACOSOG
text
Patient Study ID
Patient Initials
Institution Number
Institution Name
Data amended
boolean
Assessment Date
date
HospitalizationReportPeriodInd-2
Unnamed3
CommonTerminologyCriteriaforAdverseEventsVersion4.0LowLevelTermName
Primary Site MedDRA Code
float
AdverseEventSeverityGrade
CTC Adverse Event Attribution Category
AdverseEventReportInd-3
Surgical Complication
AdverseEventCurrentAssessmentInd